United Kingdom MHRA device registration 203201

Assisted reproduction embryo-assessment software

United Kingdom·General Medical Device·Kai Health, Inc·Registered Nov 26, 2024

Registration details

Device ID: 203201
MHRA Reference Number: 203201
Date Registered: Nov 26, 2024
Last Updated: Oct 17, 2024

Device classification

Device Type: General Medical Device
Devices: Assisted reproduction embryo-assessment software
Type: Class I

Manufacturer

Name: Kai Health, Inc
Address: B2-Google Startups Campus, 417, Yeongdong- daero, Gangnam-gu,
Seoul,, South Korea
Created Date: Oct 16, 2024

Authorized Representative

Name: CMC Medical Devices LTD
Relationship Type: UK Responsible Person
Address: Office 32 19-21 Crawford Street
London, United Kingdom
Postcode: W1H 1PJ

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About this record

Assisted reproduction embryo-assessment software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 203201. The device is manufactured by Kai Health, Inc from South Korea, classified as General Medical Device. The authorized representative in the UK is CMC Medical Devices LTD.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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